Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584912Generated: October 25, 2026

Hydrogen Peroxide → 3,5-dichloro-4-(2-(3-cyclopentyloxy-4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxide

https://huagongshe.com/reaction/1584912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant3-Cyclopentyloxy-4-methoxyphenyl 3,5-dichloropyrid-4-ylmethyl ketoneHCID 21469578—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product3,5-dichloro-4-(2-(3-cyclopentyloxy-4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxideHCID 21187845—

Reaction Conditions

Temperature80 °C

Reaction Steps

Aqueous 27.5% hydrogen peroxide (0.32 mL) is added to a solution of 3-cyclopentyloxy-4-methoxyphenyl 3,5-dichloropyrid-4-ylmethyl ketone (990 mg) in glacial acetic acid (13 mL). The. reaction is heated at 80° C. for 8 hours then allowed to stand overnight at room temperature. A further aliquot of aqueous 27.5% hydrogen peroxide (0.32 mL) is added and the mixture heated at 80° C. for 2 hours. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with saturated aqueous sodium bicarbonate until the washings remained basic. The mixture is washed with brine (50 mL), dried (MgSO4), concentrated and the residue recrystallized from a mixture of dichloromethane/ethyl acetate/heptane to give 3,5-dichloro-4-(2-(3-cyclopentyloxy4-methoxyphenyl)-2-oxoethyl)pyridine-N-oxide as a yellow solid, m.p. 179-180° C. [Elemental analysis: C,57.3; H,4.81; N,3.54; Cl,18.0%; calculated for C19H19Cl2NO4 : C,57.59; H,4.83; N,3.53; Cl,17.89%.]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935978
Source datasetuspto-grants-1999_08
ORD IDord-03be0de7de144b4284a6984767c5a0be
Source noteuspto-grants-1999_08